POYGIK SALINE

Manufacturer: Guangzhou Jinsheng Biotechnology Corporation
Effective date: 2025-12-29
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: monthly-update
Hydrated at: 2026-06-03 17:46:44

Label at a glance#

ProductPOYGIK SALINE

Active ingredientWATER

Label structure12 sections

Dosage and administration

Pour the cleansing solution directly onto the affected area to clean.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

USP Water 99.1%

OTC - ASK DOCTOR SECTION

Consult your doctor or pharmacist before use if you:
1. Have allergies, redness, or other symptoms.
2. Are preparing for pregnancy or have serious wounds.
If you are pregnant or breastfeeding, please consult your doctor or
pharmacist before use.

Use caution when using this product:

OTC - DO NOT USE SECTION

1. Do not use if the bottle is cracked.

2. Do not use if there is a foreign body inside.

Other Information:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If you are pregnant or breastfeeding, please consult your doctor or pharmacist before use

Purpose

OTC - PURPOSE SECTION

In case of overdose, seek medical help or
contact a poison control center immediately.

Other Information:

OTC - QUESTIONS SECTION

In case of overdose, seek medical help or contact a poison control center immediately.

Discontinue use and consult your doctor if you:

OTC - STOP USE SECTION

1. Experience discomfort or allergic symptoms.
2. Notice that the wound is aggravated after use.

Directions for Use:

WARNINGS SECTION

Pour the cleansing solution directly onto the affected area to clean.

DOSAGE & ADMINISTRATION SECTION

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sodium Chloride 0.9%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image description

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

POYGIK SALINE
Water
SODIUM CHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85797-102	85797-102-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM CHLORIDE	451W47IQ8X	IACT
WATER	059QF0KO0R	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
4712fc88-f372-3774-e063-6294a90a0337			3a964924-b37a-a391-e063-6294a90a1d0a	2025-12-29	Warnings	Exact identifier spl id: 4712fc88-f372-3774-e063-6294a90a0337 spl set id: 3a964924-b37a-a391-e063-6294a90a1d0a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.